FADS2 c.744+1920T>A

Variant ID: 11-61617676-T-A

NM_004265.3(FADS2):c.744+1920T>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Deciphering regulatory DNA sequences and noncoding genetic variants using neural network models of massively parallel reporter assays.

Plos One
Movva, Rajiv R; Greenside, Peyton P; Marinov, Georgi K GK; Nair, Surag S; Shrikumar, Avanti A; Kundaje, Anshul A
Publication Date: 2019

Variant appearance in text: rs174591
PubMed Link: 31206543
Variant Present in the following documents:
  • Main text
  • pone.0218073.pdf
View BVdb publication page



Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.

Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24

Variant appearance in text: rs174591
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page